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** = Publikationen gelistet in SCI/SSCI/Pubmed

** Gaksch, L; Kashofer, K; Heitzer, E; Quehenberger, F; Daga, S; Hofer, S; Halbwedl, I; Graf, R; Krisper, N; Hoefler, G; Zebisch, A; Sill, H; Wölfler, A Residual disease detection using targeted parallel sequencing predicts relapse in cytogenetically normal acute myeloid leukemia.
Am J Hematol. 2018; 93(1):23-30 Doi: 10.1002/ajh.24922 [OPEN ACCESS]
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** Binder, E; Rohrer, T; Denzer, C; Marg, W; Ohlenschlager, U; Schenkenhuber, H; Schierloh, U; Skopnik, H; Fröhlich-Reiterer, E; Bollow, E; Hofer, S; Holl, RW; Prinz, N Celiac Screening in Children and Adolescents with Diabetes mellitus Type I - Is Genotyping of celiac-specific HLA-Markers used as a Screening Method?
WIEN KLIN WOCHENSCHR. 2017; 129: 179-179.-45. Jahrestagung der Österreichischen Diabetesgesellschaft, 16.-18. November 2017; Salzburg ; Nov 16-18, 2017; Salzburg. [Oral Communication]
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** Gaksch, L; Kashofer, K; Heitzer, E; Daga, S; Hofer, S; Krisper, N; Hofler, G; Zebisch, A; Sill, H; Wolfler, A Persistence of non-DNMT3A mutations predicts relapse in cytogenetically normal AML
ONCOL RES TREAT. 2017; 40: 140-141. [Oral Communication]
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** Kojzar, H; Frohlich-Reiterer, E; Mader, J; Hofer, S; Rami-Merhar, B; de Beaufort, C; Acerini, CL; Campell, F; Kapellen, T; Hovorka, R KidsAP - The artificial pancreas in children aged 1 to 7 years with type 1 diabetes
WIEN KLIN WOCHENSCHR. 2017; 129: 162-162.-45. Jahrestagung der Österreichischen Diabetesgesellschaft; Nov 16-18; Salzburg. [Oral Communication]
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** Wenzl, K; Hofer, S; Troppan, K; Lassnig, M; Steinbauer, E; Wiltgen, M; Zulus, B; Renner, W; Beham-Schmid, C; Neumeister, P; Deutsch, A Higher incidence of the SNP Met 788 Ile in the coding region of A20 in diffuse large B cell lymphomas.
Tumour Biol. 2016; 37(4):4785-4789 Doi: 10.1007/s13277-015-4322-1 [OPEN ACCESS]
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** Gaksch, L; Kashofer, K; Heitzer, E; Daga, S; Hofer, S; Krisper, N; Höfler, G; Zebisch, A; Sill, H; Wölfler A Persitence of non-DNMT3A mutations predicts relapse in cytogenetically normal AML.
Oncol Res Treat 2016. 2016; 39(suppl3):140--Jahrestagung DGHO; OCT 14-18,2016; Leipzig. (ISBN: 2296-5270 ) [Oral Communication]
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** Schulz, E; Lind, K; Renner, W; Petersen, BS; Dill, C; Hofer, S; Lal, R; Quehenberger, F; Stolzel, F; Sill, H THE HOMOZYGOUS TP53 P72R SNP IS ASSOCIATED WITH NON-FAVORABLE CYTOGENETIC RISK GROUPS IN ACUTE MYELOID LEUKEMIA
HAEMATOLOGICA. 2016; 101: 383-383. [Poster]
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** Hackl, H; Steinleitner, K; Lind, K; Hofer, S; Tosic, N; Pavlovic, S; Suvajdzic, N; Sill, H; Wieser, R A gene expression profile associated with relapse of cytogenetically normal acute myeloid leukemia is enriched for leukemia stem cell genes.
Leuk Lymphoma. 2015; 56(4):1126-1128 Doi: 10.3109/10428194.2014.944523 [OPEN ACCESS]
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** Hofer, S; Binder, E; Loinger, M; Steichen, E; Meraner, D; Loacker, L; Weigel, G; Muhlbacher, A; Edlinger, M; Muller, T; Frohlich-Reiterer, E Prevalence of specific celiac disease of HLA Genotypes in Children and Adolescents with Type 1 Diabetes mellitus
WIEN KLIN WOCHENSCHR. 2015; 127: S154-S154.
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** Olipitz, W; Lind, K; Monsberger, N; Katschnig, A; Mangerich, A; Hofer, S; Schulz, E; Quehenberger, F; Schlembach, D; Robier, C; Woelfler, A; Zebisch, A; Sill, H Base Excision Repair Glycosylase Activity Is Impaired in a Subgroup of Acute Myeloid Leukemia Resulting in Increased Levels of Oxidative Base Lesions
BLOOD. 2014; 124(21):-56th Annual Meeting of the American-Society-of-Hematology; DEC 06-09, 2014; San Francisco, CA. [Poster]
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** Olipitz, W; Lind, K; Monsberger, N; Katschnig, A; Mangerich, A; Hofer, S; Schulz, E; Quehenberger, F; Schlembach, D; Robier, C; Wölfler, A; Zebisch, A; Sill, H Base excision repair glycosylase activity is impaired in a subgroup of acute myeloid leukemia resulting in increased levels of oxidative base lesions
Oncol Res Treat. 2014; 37(S5):49-49.-Annual Meeting of the German, Austrian and Swiss Associations of Hematology and Medical Oncology; OCT 10-14; Hamburg, GERMANY. (ISBN: 978-3-318-02811-9 ) [Poster]
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** Schulz, E; Klampfl, P; Holzapfel, S; Janecke, AR; Ulz, P; Renner, W; Kashofer, K; Najima, S; Leitner, A; Zebisch, A; Wölfler, A; Hofer, S; Gerger, A; Lax, S; Beham-Schmid, C; Steinke, V; Geigl, JB; Höfler, G; Speicher, MR; Boland, CR; Kumanogoh, A; Sill, H Germline variants in the semaphorin SEMA4A confer susceptibility to familial colorectal cancer type X
Oncol Res Treat. 2014; 37(S5):105-105.-Annual Meeting of the German, Austrian and Swiss Associations of Hematology and Medical Oncology; OCT 10-14, 2014; Hamburg, GERMANY. (ISBN: 978-3-318-02811-9 ) [Oral Communication]
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